1. A Locus for Autosomal Dominant Hereditary Spastic Ataxia, SAX1,Maps to Chromosome 12p13 
I.A. Meijer, C.K. Hand, K.K. Grewal, M.G. Stefanelli, E.J. Ives, G.A. Rouleau 
The American Journal of Human Genetics 
Volume 70, Issue 3, Pages (March 2002)
DOI: /338933
Copyright © 2002 The American Society of Human Genetics Terms and Conditions

2. Figure 1
Informative section of family 71, with the chromosome 12p13 haplotype. The disease haplotype for HSA is indicated by the blackened bar. Affected individuals are indicated by blackened symbols, unaffected individuals are indicated by unblackened symbols, and key recombinants (VI:4 and VI:13) are indicated by an asterisk (*). These recombinants determined the critical interval to be 10 cM, flanked by markers D12S1685 and GATA151H05.
The American Journal of Human Genetics  , DOI: ( /338933)
Copyright © 2002 The American Society of Human Genetics Terms and Conditions

3. Figure 2
Informative section of family 13, with the chromosome 12p13 haplotype. The disease haplotype for HSA is indicated by the blackened bar. Affected individuals are indicated by blackened symbols, unaffected individuals are indicated by unblackened symbols, key recombinants (V:14 and VI:11) are indicated by an asterisk (*), and possibly affected individuals are indicated by a question mark (?). These recombinants determined the critical region to be 8 cM, flanked by markers D12S1725 and D12S397.
The American Journal of Human Genetics  , DOI: ( /338933)
Copyright © 2002 The American Society of Human Genetics Terms and Conditions

4. Figure 3
Informative section of family 27, with the chromosome 12p13 haplotype. The disease haplotype for HSA is indicated by the blackened bar. Affected individuals are indicated by blackened symbols, and unaffected individuals are indicated by unblackened symbols. Individual III:4 shares the complete haplotype and is unaffected.
The American Journal of Human Genetics  , DOI: ( /338933)
Copyright © 2002 The American Society of Human Genetics Terms and Conditions